NM_001018005.2(TPM1):c.153G>A (p.Lys51=) AND Hypertrophic cardiomyopathy
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Apr 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000629090.9
Allele description [Variation Report for NM_001018005.2(TPM1):c.153G>A (p.Lys51=)]
NM_001018005.2(TPM1):c.153G>A (p.Lys51=)
Condition(s)
- Name:
- Hypertrophic cardiomyopathy
- Synonyms:
- HYPERTROPHIC MYOCARDIOPATHY
- Identifiers:
- MONDO: MONDO:0005045; MeSH: D002312; MedGen: C0007194; Human Phenotype Ontology: HP:0001639
-
Homo sapiens cDNA FLJ52732 complete cds, moderately similar to Zinc finger prote...
Homo sapiens cDNA FLJ52732 complete cds, moderately similar to Zinc finger protein 418gi|194386685|dbj|AK299091.1|Nucleotide
-
DB066632 TESTI4 Homo sapiens cDNA clone TESTI4008031 5', mRNA sequence
DB066632 TESTI4 Homo sapiens cDNA clone TESTI4008031 5', mRNA sequencegi|83549640|gnl|dbEST|34573125|dbj| 632.1|Nucleotide
-
dc32a12.x1 NICHD_XGC_Emb3 Xenopus laevis cDNA clone IMAGE:3398782 3', mRNA seque...
dc32a12.x1 NICHD_XGC_Emb3 Xenopus laevis cDNA clone IMAGE:3398782 3', mRNA sequencegi|9709151|gnl|dbEST|5688546|gb|BE5 .1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024